supply of dual chamber implantable cardioverter defibrillator pulse generator system:dual chamber implantable cardioverter defibrillator pulse generator system:,82278033-dual chamber implantable cardioverter defibrillator pulse generator system: system should have advanced features for the reliable detection and m anagement of ventricular tachycardia and ventricular fibrillation, including features to differentiate supra-ventricular tachycardia from ventricular tachycardia and features to avoid inappropriate shocks, tiered therapy delivery, choice of atp protocols and shock ene rgies, and should be capable of delivering maximum energy of 35j or more and should have features for management of high defibrillation energy requirement. charge times should b e within clinically acceptable limits throughout the lifetime of the device. should have fea tures for automatically alerting the patient in the event of a battery or lead fault. data s torage, retrieval and display should be efficient and user friendly. data storage should in clude episode details, therapy delivered and results and electrogram storage and should be comprehensive. bradycardia pacing (including independently programmable parameters f or high output for post-shock pacing) should be available. warranty terms should be speci fied clearly along with the quotation. firms should submit detailed literature of the item i n a bulletin/tutorial format which should contain all the details about the product. comp liance statement of each specification to be submitted. the firm quoting the tender should submit a letter of authorisation from the principal firm/original equipment manufacturer. the manufacturer / supplier should submit proof of supply to a major government institute. the safety and efficacy of the icd device in clinical use should be documented in scientific p ublications. all the above mentioned specifications are essential and mandatory and shoul d be submitted at the time of initial tender submissi